FAQ: CSV, CSA, and Why the Paradigm Shift This FAQ curates many questions from our customers and attendees to our various webinars with the FDA on the CSA Guidance. 0 Sandy Hedberg - February 2, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory
Key differences in the requirements for SFDA UDI and US & EU UDI Blog article topic: Key differences in the requirements for SFDA UDI and US & EU UDI. 0 Jay Crowley - January 29, 2022 Blogs Medical Device Manufacturing, Regulatory
Q&A: UDI Registration in EUDAMED Blog article written from the Q&A during the UDI Registration in EUDAMED webinar. 0 Jay Crowley - January 29, 2022 Blogs Medical Device Regulatory, Safety
FDA Perspectives on Cloud Technologies Video on FDA Perspectives on Cloud Technologies. 0 Jim Macdonell - January 28, 2022 Videos Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
Your Compliance and Technology Today Video on Your Compliance and Technology Today. 0 Roger Davy - January 28, 2022 Videos Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
Medical Device Company Updates 450 QMS SOPs in time for EU MDR Case study on Medical Device Company Updates 450 QMS SOPs in time for EU MDR. Jim Macdonell - January 21, 2022 Case Studies Medical Device Regulatory, Safety
